Home NDC 81772-007 NDC 81772-007 - CLOBETASOL PROPIONATE This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 81772-007
Package NDCs from labels 81772-007-01
Manufacturer Bora Pharmaceuticals Ophthalmic Inc. Taoyuan plant | Bora Pharmaceuticals Ophthalmic Inc. Taoyuan plant, Research Building
Effective date 2024-10-08
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type CLOBETASOL PROPIONATE Bora Pharmaceuticals Ophthalmic Inc. Taoyuan plant | Bora Pharmaceuticals Ophthalmic Inc. Taoyuan plant, Research Building 2024-10-08 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81772-007 CLOBETASOL PROPIONATE SUSPENSION/ DROPS [BORA PHARMACEUTICALS OPHTHALMIC INC. TAOYUAN PLANT] 1 Unmatched 20241018_2405ed5b-e7f0-a51c-e063-6394a90a8b1e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 90 of 136 · 2,704 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.